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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience(MAUDE)
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35 records meeting your search criteria returned- Product Code: MGB Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
CORDIS CORPORATION EXOSEAL 08/20/2024
CORDIS US CORP EXOSEAL 05/09/2024
ABBOTT VASCULAR INC. PERCLOSE PROSTYLE 10/19/2022
CORDIS SANTA CLARA MYNX CONTROL VCD 5F 10/04/2021
CORDIS SANTA CLARA MYNXGRIP VASCULAR CLOSURE DEVICE 5F 11/22/2020
CORDIS CORPORATION VASCULAR CLOSURE DEVICE 7F - 03/23/2020
CORDIS SANTA CLARA MYNXGRIP VASCULAR CLOSURE DEVICE 5F 09/02/2019
TERUMO MEDICAL CORPORATION 6FR ANGIO-SEAL STS PLUS VASCULAR CLOSURE 06/18/2018
CORDIS SANTA CLARA MYNXGRIP VASCULAR CLOSURE DEVICE 5F 05/23/2018
CORDIS CORPORATION EXOSEAL VASC. CLOS.DEV.F7 05/21/2018
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